Disease #06757 (OZEMA5;OOMD (ocyte/zygote/embryo maturation arrest, type 5), OMIM:617996)

Official abbreviation OZEMA5;OOMD
Name ocyte/zygote/embryo maturation arrest, type 5
OMIM ID 617996
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene WEE2
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited 2024-11-08 11:48:51 +01:00 (CET)

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